Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

40 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
[Congenital heart diseases in women].
Putotto C, Unolt M, Caiaro A, Marino D, Massaccesi V, Marino B, Digilio MC. Putotto C, et al. Among authors: unolt m. G Ital Cardiol (Rome). 2013 Feb;14(2):120-5. doi: 10.1714/1218.13524. G Ital Cardiol (Rome). 2013. PMID: 23389314 Review. Italian.
Transposition of great arteries: new insights into the pathogenesis.
Unolt M, Putotto C, Silvestri LM, Marino D, Scarabotti A, Valerio Massaccesi, Caiaro A, Versacci P, Marino B. Unolt M, et al. Front Pediatr. 2013 Jun 6;1:11. doi: 10.3389/fped.2013.00011. Front Pediatr. 2013. PMID: 24400257 Free PMC article. Review.
Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.
Unolt M, DiCairano L, Schlechtweg K, Barry J, Howell L, Kasperski S, Nance M, Adzick NS, Zackai EH, McDonald-McGinn DM. Unolt M, et al. Am J Med Genet A. 2017 Jan;173(1):135-142. doi: 10.1002/ajmg.a.37980. Epub 2016 Sep 28. Am J Med Genet A. 2017. PMID: 27682988
Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements.
Demaerel W, Hestand MS, Vergaelen E, Swillen A, López-Sánchez M, Pérez-Jurado LA, McDonald-McGinn DM, Zackai E, Emanuel BS, Morrow BE, Breckpot J, Devriendt K, Vermeesch JR; International 22q11.2 Brain and Behavior Consortium. Demaerel W, et al. Am J Hum Genet. 2017 Oct 5;101(4):616-622. doi: 10.1016/j.ajhg.2017.09.002. Epub 2017 Sep 28. Am J Hum Genet. 2017. Retraction in: Am J Hum Genet. 2018 Sep 6;103(3):457. doi: 10.1016/j.ajhg.2018.08.011. PMID: 28965848 Free PMC article. Retracted.
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.
Unolt M, Versacci P, Anaclerio S, Lambiase C, Calcagni G, Trezzi M, Carotti A, Crowley TB, Zackai EH, Goldmuntz E, Gaynor JW, Digilio MC, McDonald-McGinn DM, Marino B. Unolt M, et al. Am J Med Genet A. 2018 Oct;176(10):2087-2098. doi: 10.1002/ajmg.a.38662. Epub 2018 Apr 16. Am J Med Genet A. 2018. PMID: 29663641 Free PMC article. Review.
40 results